Ingestible, high density, compressed-tablet fiber-composition

ABSTRACT

An ingestible, high-density compressed-tablet fiber-composition having a high dietary fiber content is prepared by blending at least one high fiber source with a microcrystalline cellulose compression aid; mixing water with the blend at a rate ratio of about 1.5:1 to about 2.5:1 based on the weight of water to the weight of the blend, for a time sufficient to form a cohesive, deformable, plastic mass; drying the plastic mass and milling the dried product to recover granules having a particle size of about 125 to about 840 microns; blending the granules with a tableting lubricant and compressing into a high-density, high fiber tablet.

FIELD OF THE INVENTION

The present invention relates to an ingestible, high density,compressed-tablet fiber-composition and method for the preparationthereof. More particularly, this invention relates to a high density,compressed-tablet fiber-composition prepared by controlling certainsteps in a wet granulation tableting operation to permit the formationof a compressed tablet fiber composition having a high density and ahigh dietary fiber content, which is of sufficient hardness to withstandthe mechanical abrasion encountered in packaging, shipping and use. Thecompressed tablet composition of this invention may be prepared inswallowable or chewable form. The high density and high dietary fiberfeature of the invention is especially advantageous is swallowablecompressed tablets where the size of the tablet is necessarily limited.Chewable compressed tablets prepared according to the method of thisinvention have an advantage in that they are palatable and substantillyfree of the dry, dusty mouthfeel generally associated with dietary fiberproducts. Thus, the convenient form and pleasant taste of the highdensity, compressed-tablet fiber-composition prepared according to themethod of this invention encourages consumers to adhere to recommendeddietary programs.

BACKGROUND OF THE INVENTION

Since the early 1970's, the importance of fiber in health and diseasehas received an increasing amount of attention from consumers. Researchto date has provided a body of evidence which enhances the role of fiberin human metabolism. In preventative medicine applications, fiber hasbeen mentioned as having possible value in a variety of areas, amongwhich there may be mentioned constipation, weight reduction,diverticulitis, cardiovascular disease, and cancer. As a result,considerable efforts have been expended in the development offiber-containing foods and snacks. Although there are many physiologicalclaims to the benefits of dietary fiber, since different fibercomponents have very different physiological functions, the daily levelof dietary fiber recommended to achieve a particular physiologicaleffect will vary wih the type of fiber ingested. Additionally, sincedietary fiber products characteristically have an unpleasant taste andmouthfeel, a relatively low amount of fiber is present in such productsin relation to the other food or snack ingredients. Thus, ingestion oflarge amounts of currently available fiber-containing foods or snacks isgenerally required in order to attain a sufficient level of fiber withinthe body to achieve a particular physiological function.

Ideally, a tablet containing a high amount of dietary fiber which can bechewed or swallowed several times a day as, for example, before andafter meals, would be most advantageous in maintaining a desired levelof fiber in the diet. Attempts have been made in the past to preparehigh-fiber tableted compositions. U.S. Pat. No. 4,565,702 disclosesdietary food products which can be formed into gelatin tabletscontaining dietary fiber. Belgium Pat. No. 881,168 discloses a highprotein dietary product containing some fiber prepared in the form of atablet, but this tablet is a heat-treated, molded article.

In a broad sense, tablets may be classified according to their method ofmanufacture, i.e., molded tablets or compressed tablets. Molded tabletsor tablet triturates, originally made from moist materials in atriturate, mold, can now usually be made on table machines, generally insmall scale operations. Compressed tablets, on the other hand, are themost widely used dosage form since they are convenient to use, deliverthe intended dose with a high degree of accuracy, and are capable ofbeing produced by large scale processes. Among the methods for preparingcompressed tablets, the wet granulation method is the most popular dueto the increased probability that the granulation will meet all thephysical requirements for compression into good tablets. Well madecompressed tablets possess certain attributes, among which there may bementioned sufficient strength to withstand handling and shipping priorto use, freedom from defects such as cracks and chipped edges,reasonable storage stability and the ability to release activeingredients in a reproducible and predictable manner. Thus, althoughmuch is known concerning the methods for obtaining high-qualitycompressed tablets, the prior art does not disclose the preparation ofhigh-density, compressed-tablet fiber-compositions.

SUMMARY OF THE INVENTION

This invention relates to a method for preparing an ingestible,high-density, compressed-tablet fiber-composition having a high dietaryfiber content. The compressed tablet is prepared by a uniquemodification of the traditional wet granulation procedure for preparingtablets. In particular, at least one high-fiber source is blended with amicrocrystalline cellulose compression aid to form a homogenous blend.Water is then mixed with the blend in a weight ratio of about 1.5:1 toabout 2.5:1, based on the weight of water to the weight of the blend,for a time sufficient to form a cohesive, deformable, plastic mass. Theplastic mass is then dried to a moisture content of less than about 8%by weight, based on the weight of the dried material. The dried productis milled to recover granules having a particle size of about 125 toabout 840 microns. The granules are then blended with a tabletinglubricant and compressed into a high-density, fiber tablet having adietary fiber content of about 30% to about 95% by weight, based on thetotal weight of the compressed-tablet fiber-composition. It is criticalto the success of the invention that the above steps be followed inorder to obtain a high-density compressed tablet having a high fibercontent and appropriate hardness.

DETAILED DESCRIPTION OF THE INVENTION

The first step in the method for preparing the ingestible, high density,compressed-tablet fiber-composition in accordance with this inventioninvolves the blending of at least one high fiber source with amicrocrystalline cellulose compression aid to form a homogeneous blend.The term "blend" is meant to include the fiber from the high-fibersource and the microcrystalline cellulose. The term "dietary fiber" isunderstood to mean that part of plant material in the diet which isresistant to digestion by the secretions of the human gastrointestinaltract. Dietary fiber can consist of variable proportions of complexcarbohydrates such as cellulose, pentosans, and uronic acids, as well aslignin. Fiber materials, wherein the dietary fiber content is at least60%, preferably 70% or more, are suitable as the high-fiber source inthe practice of this invention. A technique for determining dietaryfiber content is described in "Total Dietary Fiber: AOAC CollaborativeStudy," Jan. 25, 1982, incorporated herein by reference. This techniqueutilizes enzymatic and chemical procedures to isolate the dietary fiber.When a wheat bran or corn bran for example, is treated according to thisAOAC method the recoverable dietary fiber is an insoluble fiber. Thebran is first treated with a solvent, e.g., petroleum ether or hexane,to remove the fat. The defatted bran is then digested enzymatically withprotease. Finally, the bran is treated with α or β-amylase andamyloglucosidase. The recoverable material is protein-free, fat-free andcarbohydrate-free insoluble dietary fiber. Thus the recovered materialis essentially non-digestible fiber, free of any association or residueof digestibles.

In the initial blending with the microcrystalline cellulose, about 20%to about 90%, preferably about 20% to about 80%, most preferably about25% to about 75% dietary fiber from the high fiber source, based on thetotal weight of the compressed-tablet fiber-composition, is included. Itis desirable to utilize as the high fiber source in the practice of thisinvention, fiber derived from fruits and grains. Thus, fiber derivedfrom the following materials: tree fruits including the apple, apricot,cherry, peach, pear, plum and the like; fiber derived from citrus fruitssuch as the lemon, lime, orange, grapefuit and the like; or fiberderived from bushberries, including the blackberry, raspberry,strawberry, blueberry and the like, are representative suitable fruitfiber sources. Fiber derived from cereal grains such as barley, corn(maize), oats, rice, rye and wheat, are representative suitable grainfiber sources. Fiber derived from other sources such as vegetable fiberand cellulose fiber are also suitable for use in the practice of thisinvention. Among the previously mentioned fiber sources those having ahigh concentration of dietary fiber such as apple, pear, barley, oat,and corn fiber are preferred. It is especially preferred in the methodof this invention to use, as the high-fiber source, a combination of afruit fiber and a grain fiber. In the preparation of a chewable tabletwhere taste considerations are important, a combination of apple fiberand corn bran is especially preferred as the high-fiber source.

The microcrystalline cellulose compression aid which is blended with thehigh-fiber source is a purified, partially depolymerized celluloseprepared by treating alpha-cellulose obtained as pulp from fiberousplant material with mineral acids, as is more fully described in theOfficial Monographs of the United States Pharmacopia. Microcrystallinecellulose in amounts of about 5% to about 75%, preferably about 7% toabout 50% by weight, based on the total weight of the compressed-tabletfiber-composition, is sufficient to function as a compression aid. Sincethe microcrystalline cellulose is considered a fiber, it also serves, inthe method of this invention, as both a compression aid during theformation of the compressed tablet and as a fiber. Thus, the totaldietary fiber content of the tableted composition of this invention,including dietary fiber from the high fiber source and from themicrocrystalline cellulose compression aid ingredient, is about 30% toabout 95%, preferably from about 35% to about 90%, by weight, based onthe total weight of the compressed-tablet fiber-composition.

Following the blending of the high-fiber source and the microcrystallinecellulose compression aid, water is mixed with the blend. A traditionalwet granulation procedure, as described in Remington's PharmaceuticalScience, 17th Edition, 1985, involves weighing, mixing, granulation,screening the damp mass, drying, dry screening, lubrication andcompression. Following weighing and mixing, a solution of a bindingagent is added to the mixed powders. The powder mass is wetted with thebinding solution until the mass has the consistency of damp snow orbrown sugar. If the granulation is over-wetted, the granules will behard, requiring considerable pressure to form tablets, and the resultanttablets will have a mottled appearance. If the powder mixture is notwetted sufficiently, the resulting granules will be too soft, breakingdown during lubrication and causing difficulty during compression.

Other references have characterized the end point in the wet granulationprocess somewhat differently. For example, in Volume 1 of"Pharmaceutical Dosage Forms: Tablets," published by Marcel Dekker,Inc., New York 1980, the end point is described as follows: the wet massproduced by mixing a liquid with the solid ingredients should have adough-like consistency so that a handful can be formed into a shapewithout crumbling. When pressed into a ball with the hands and broken inhalf, the wet mass should give a clean fracture without sticking orcrumbling. If the mass has a tendency to stick or not break clean, thegranulation is usually too wet. If the mass crumbles or breaks intopieces, it is too dry. In the "Theory and Practice of IndustrialPharmcy", 2nd Edition, published by Lea & Febiger, Philadelphia, 1976,it is stated that a rough way to determine the end point in a wetgranulation process is to press a portion of the wet mass in the palm ofthe hand and if the ball crumbles under moderate pressure, the mixtureis ready for the next stage in processing, which is wet screening.

Quite surprisingly, it has been found that in the practice of thesubject invention, it is necessary to go beyond the above describedend-points in the wet granulation process in order to obtain, as a finalproduct, a compressed tablet having suitable density and hardness. Moreparticularly, water is mixed with the blend of the high-fiber source andthe microcrystalline cellulose compression aid at a weight ratio ofabout 1.5:1 to about 2.5:1, based on the weight of water to the weightof the blend, for a time sufficient to form a cohesive, deformable,plastic mass. The plastic mass obtained would be considered over-wettedin terms of the aforementioned end point description as damp snow orbrown sugar. Moreover, if the over-wetted plastic mass of this inventionis pressed into a ball and broken in half, it does not give a cleanfracture nor does it crumble. Rather, the plastic mass is deformable andtears apart rather than breaking apart with a clean fracture. Thus, thecohesive, deformable, plastic mass of this invention, which isover-wetted in terms of a traditional wet granulation process, is formedby adding water to the dry blend in the above stated ratio and mixinguntil the desired critical physical form is obtained. As seen incomparative Examples IV and V, if the weight ratio of water to the blendis above or below 1.5:1 to 2.5:1, tablets of insufficient hardness areobtained. The mixing time is also critical in that, if mixing iscontinued beyond the formation of the cohesive, deformable, plasticmass, heat is built up, water is lost through evaporation, and the massbecomes too dry. The length of mixing time depends to a large extent onthe efficiency of the mixing apparatus being used, but msut be continueduntil the desired physical form, as described above, is obtained.Generally, mixing times of about 10 to about 40 minutes, preferablyabout 15 to about 25 minutes, depending upon the type of mixingequipment is used, have been found to be suitable to obtain the desiredphysical form.

At this point in a traditional wet granulation process, the granulationis wet screened to obtain coarse, granular aggregates which are thendried. Quite surprisingly, it has been discovered that the wet screeningstep used in traditional wet granulation processes is not essential tothe practice of this invention. Rather, the over-wetted cohesive,deformable, plastic mass is dried directly, without wet screening, to amoisture content of less than about 8%, preferably less than about 5%,by weight, based on the weight of the dried material. The elimination ofthe time-consuming, expensive wet screening step provides a considerableadvantage in large scale commercial tableting operations. However, thewet screening step of the traditional wet granulation process may beincluded in the method of this invention, in which case the wet screenedgranules are also dried to the above stated moisture content. In eithercase, the dried product is then milled to recover granules having aparticle size of from about 125 to about 840 microns. For thepreparation of chewable tablets wherein taste is a consideration, thegranules should have a particle size of about 210 to about 840 microns,preferably about 250 to about 840 microns. In the preparation of aswallowable tablet where bulk density, compressability and tablet sizeare the primary considerations, milling to recover granules having aparticle size of about 125 to about 710 microns, preferably about 149 toabout 590 microns is desired.

The next step in the method of preparing the ingestible, high density,compressed-tablet fiber-composition in accordance with this invention isthe blending of a tableting lubricant with the aforementioned milledgranules. Traditionally, lubricants are added to tablet granulations fora number of reasons, including to improve the rate of flow of the tabletgranulation, to limit the wear on dies and punches, to prevent adhesionof the tablet material to the surface of the dies and punches, to reduceinterparticle friction, and to facilitate the ejection of tablets fromthe die cavity. The lubricants useful in the method and compositions ofthis invention are among those well-known in the art. Representativeexamples of such lubricants include stearic acid, metallic stearates,hydrogenated vegetable oils, partially hydrogenated vegetable oils,animal fats (e.g. triglycerides), modified maltodextrins, polyethyleneglycol, light mineral oil, sodium benzoate and mixtures thereof. Amongaforementioned lubricants, stearic acid, hydrogenated vegetable oils,partially hydrogenated vegetable oils, animal fats and modifiedmaltodextrins are preferred. The quantity of lubricant used in themethod of this invention will vary with the lubricant selected and withthe fiber composition being tableted. Generally, from about 0.01% toabout 5%, preferably about 0.05% to about 3.5%, by weight of lubricant,based on the total weight of the compressed-tablet fiber-composition,has been found to be sufficient to facilitate tableting operations inthe method of this invention. In an alternate embodiment of the methodof this invention, a portion of the tablet lubricant may be added to theinitial blend of the high fiber source and the microcrystallinecellulose, with the remainder of the tablet lubricant being mixed withthe milled granules just prior to compression into tablet form.

As a final step in the method of this invention, the blend of the tabletlubricant and granules of high fiber source and microcrystallinecellulose are compressed into tablet form, following conventionaltableting techniques well-known in the art. The basic mechanical unit intablet compression involves the operation of two steel punches within asteel die cavity. The tablet is formed by the pressure exerted on thegranulation by the punches within the die cavity. The tablet assumes thesize and shape of the punches and die used. The simplest tabletingmachines available are those having a single punch design which produceone tablet at a time. The majority of single punch tablet machines arepower-driven and heavier models are capable of high pressures. Forincreased production, rotary tablet machines offer great advantages. Ahead carrying a number of sets of punches and dies revolves continuouslywhile the tablet granulation runs from the hopper through a feed frameand into the dies placed in a large, steel plate revolving under thefeed frame. Compression takes place as the upper and lower punches passbetween a pair of rollers. This action produces a slow squeezing effecton the material in the die cavity from the top and bottom and thusproviding an opportunity for entrapped air to escape. Adjustments forthe tablet weight and hardness can be made. High-speed rotary tabletmachines capable of compressing tablets at high production rates arecommercially available.

The resistance of a tablet to chipping, abrasion, or breakage under theconditions of storage, transportation, and handling before usage dependson the hardness of the table. The Strong-Cobb hardness tester measuresthe diametrically applied force required to break a tablet. In thisinstrument, the force is produced by a manually operated air pump. Asthe pressure is increased, a plunger is forced against a tablet placedon an anvil. The final breaking point is indicated on a dial calibratedto 30 arbitrary units.

In accordance with the method of this invention, ingestible,high-density, compressed-tablet fiber-compositions are obtained having ahardness of about 10 to about 28, preferably about 11 to about 22Strong-Cobb Units. Chewable compressed tablets prepared in accordancewith the method of this invention preferably have a minimum hardness ofat least about 11 Strong-Cobb Units, while swallable compressed tabletsprepared in accordance with the method of this invention preferably havea minimum hardness of at least about 15 Strong-Cobb Units.

The chewable high density, compressed-tablet fiber-composition of thisinvention preferably also contains at least one flavoring agent.Flavoring agents well-known in the food and confection art may be addedto the fiber compositions of the instant invention. These flavoringagents may be chosen from synthetic flavor oils and/or those derivedfrom natural fruits, plants, leaves, flowers, and so forth, andcombinations thereof. Representative flavors are artificial, natural orsynthetic fruit flavors such as citrus oil including lemon, orange,grape, lime and grapefruit and fruit essences including apple, apricot,strawberry, cherry, pineapple and so forth. Also useful are flavor oilssuch as spearmint oil, cinnamon oil, oil of wintergreen(methylsalicylate) and peppermint oils. The amount of flavoring agentemployed is normally a matter of preference, subject to such factors asflavor type, base type and strength desired. In general, amounts ofabout 0.05% to about 5.0% by weight of the total compressed tabletcomposition are useable, with amounts of about 0.3% to about 2.5% beingpreferred and amounts of about 0.7% to about 2.0% being most preferred.

Chewable compressed tablets prepared in accordance with the method ofthis invention preferably contain at least one sweetening agent. Thesweetening agent may be selected from a wide range of materials,including watersoluble sweetening agents, water-soluble artificialsweetners, and dipeptide based sweeteners, including mixtures thereof.Without being limited to particular sweeteners, representativeillustrations encompass:

A. Water-soluble sweetening agents such as monosaccharides,disaccharides, and polysaccharides such as xylose, ribose, glucose,mannose, galactose, fructose, dextrose, sucrose, maltose, partiallyhydrolyzed starch or corn syrup solids and sugar alcohols such assorbitol, xylitol, mannitol and mixtures thereof.

B. Water-soluble artifical sweeteners such as the soluble saccharinsalts, i.e., sodium or calcium saccharin salts, cyclamate salts,acesulfam-K and the like, and the free acid form of saccharin.

C. Dipeptide based sweeteners such as L-aspartyl-L-phenylalanine methylester and materials described in U.S. Pat. No. 3,492,131 and the like.In general, the amount of sweetener is primarily a matter of tastepreferance and will vary with the sweetener selected and with the fiberingredients in the composition being tableted. This amount will normallybe about 0.01% to about 90% by weight, depending on whether a natural orartificial sweetener is used. The water-soluble sweeteners described incategory A above are preferably used in amounts of about 25% to about75% by weight, and most preferably from about 50% to about 65% by weightof the final high-density fiber compressed tablet composition. Incontrast, the artificial sweeteners described in categories B and Cabove are generally used in amounts of about 0.005% to about 5.0%, mostpreferably about 0.05% to about 2.5% by weight, of the final compressedtablet composition. These amounts are ordinarily necessary to achieve adesired level of sweetness independent from the flavor level achievedfrom flavoring agents.

If a sweetening agent having a degree of bulk, such as one or more ofthose described in Category A above is used, it is preferable to includesuch sweetener with the initial blend of the high-fiber source and themicrocrystalline cellulose at the beginning of the wet granulationprocess. Artificial sweeteners such as those described in Category Babove may also be added with the initial blend. However, if anartificial sweetener, such as one of those described in Category C aboveis used, it is preferable to blend such sweetener with the tabletlubricant and flavor prior to the tablet compression operation.

The advantages of the instant invention can be further appreciated byreference to the following examples. These examples are intended toillustrate preferred embodiments and are by no means intended to limitthe effective scope of the claims. All percents are by weight of thefinal high density, compressed-tablet fiber-composition unless otherwisespecified.

EXAMPLE I Swallowable Tablet

Dry blend 800 grams of corn bran (75% dietary fiber), 320 grams ofmicrocrystalline cellulose and 480 grams of apple fiber (60% dietaryfiber). Add a quantity of water equal to 21/2 times the weight of theblend (4,000 grams of water). Using a planetary mixer, mix until acohesive, deformable, plastic mass is formed (about 20-25 minutes). Wetscreen using an 8 mesh screen (U.S. Standard), dry the granules untilthe moisture content is less than 4% loss on drying. Mill the driedproduct using a 30 mesh screen (U.S. Standard). Using a rotary tabletmachine and 0.380 inch by 0.625 inch elliptical tooling, form 0.765 gramtablets at a maximum pressure of 5 tons. Each tablet obtained contains73.2% total dietary fiber and has a hardness of 18-20 Strong-Cobb Units.

EXAMPLE II Chewable Tablets

Place 3.42 kilograms of corn bran (75% dietary fiber), 1.37 kilograms ofmicrocrystalline cellulose, 2.06 kilograms of apple fiber (60% dietaryfiber), 6.85 kilograms of dextrose and 6.85 grams of stearic acid in ahigh intensity mixer and mix for 5 minutes. Slowly add 13.7 kilograms ofwater over an 8 minute period while mixing. Continue mixing until acohesive, deformable, plastic mass is obtained (about 8 minutes). Dry ina forced draft oven at 80° C. to a moisture content of less than 4% losson drying. Mill using 6-10 mesh screen (U.S. Standard) to obtaingranules having a particle size of predominantly 70 mesh or coarser andplace in a planetary mixer. Add 327.6 grams of spray dried fruit flavorand 5-6 grams of stearic acid and mix for 5 minutes. Form tablets usinga rotary tablet press and 27/32 inch flat faced, beveled edged toolingat a maximum pressure of 5-6 tons. Tablets of 2.82 grams each areobtained having a dietary fiber content of 36% and a hardness of 16-18Strong-Cobb Units.

EXAMPLE III Chewable Tablets

Using a high intensity mixer mix 3500 grams of corn bran (75% dietaryfiber), 1396 grams of microcrystalline cellulose, 2104 grams of applefiber (60% dietary fiber), and 7000 grams of dextrose for 2 minutes. Add12,800 grams of water and mix until a cohesive, deformable, plastic massis formed (about 10-15 minutes). Dry for 10-12 hours at 65°-75° C. in aforced draft oven (moisture content 0.5% loss on drying.) Mill andseparate the finer than 60 mesh material from the coarser than 60 meshmaterial. Place 2752 grams of the coarser than 60 mesh material into aplanetary mixer, blend with 65.96 grams of spray dried fruit flavor for2-3 minutes. Add 2.5 grams of stearic acid and mix for 1-2 minutes. Formtablets using a rotary tablet press and 27/32 inch flat faced, bevelededge tooling, at a maximum pressure of 9-10 tons. Tablets of 2.75 gramseach are obtained having a dietary fiber content of 36% and a hardnessof 23-25 Strong-Cobb Units.

COMPARATIVE EXAMPLE IV Chewable Tablets

Using a high intensity mixer mix 3500 grams of corn bran (75% dietaryfiber), 1396 grams of microcrystalline cellulose, 2104 grams of applefiber (60% dietary fiber), and 7000 grams of dextrose for 2 minutes. Add18,000 grams of water and mix until a wet paste is formed (about 10-15minutes). Dry for 10-12 hours at 65°-75° C. in a forced draft oven(moisture content 0.5% loss on drying). Mill and separate the finer than60 mesh material from the coarser than 60 mesh material. Place 2752grams of the coarser than 60 mesh material into a planetary mixer, blendwith 65.96 grams of spray dried fruit flavor for 2-3 minutes. Add 2.5grams of stearic acid and mix for 1-2 minutes. Form tablet using arotary tablet press and 27/32 inch flat faced, beveled edge tooling, atmaximum pressure of 9-10 tons. Tablets of 2.75 grams each having adietary fiber content of 36% and a hardness of only 5-7 Strong-CobbUnits are obtained.

COMPARATIVE EXAMPLE V Chewable Tablets

Using a high intensity mixer mix 3500 grams of corn bran (75% dietaryfiber), 1396 grams of microcrystalline cellulose, 2104 grams of applefiber (60% dietary fiber), and 7000 grams of dextrose for 2 minutes. Add6000 grams of water and mix until a consistency similar to damp snow isobtained (about 10-15 minutes). Dry for 10-12 hours at 65°-75° C. in aforced draft oven (moisture content 0.5% loss on drying.) Mill andseparate the finer than 60 mesh material from the coarser than 60 meshmaterial. Place 2752 grams of the coarser than 60 mesh material, into aplanetary mixer, blend with 65.96 grams of spray dried fruit flavor for2-3 minutes. Add 2.5 grams of stearic acid and mix for 1-2 minutes. Formtablets using a rotary tablet press and 27/32 inch flat faced, bevelededge tooling at maximum pressure of 9-10 tons. Tablets of 2.75 gramseach having a dietary fiber content of 36% and a hardness of only 8-9Strong-Cobb Units are obtained.

The invention being thus described, it will be obvious that the same maybe varied in many ways. Such variations are not to be regarded as adeparture from the spirit of scope of the invention and all suchmodifications are intended to be included within the scope of theclaims.

What is claimed is:
 1. A method for preparing an ingestible, highdensity, compressed-tablet fiber-composition which comprises:(A)blending at least one high fiber source and a microcrystalline cellulosecompression aid to form a homogenous blend: (B) mixing water with theblend of step (A) at a weight ratio of about 1.5:1 to about 2.5:1, basedon the weight of water to the weight of the blend, for a time sufficientto form a cohesive, deformable, plastic mass; (C) drying the plasticmass of step (B) to a moisture content of less than abut 8% by weight,based on the weight of the dried material; (D) milling the dried productof step (C) to recover granules having a particle size of about 125 toabout 840 microns; (E) blending the granules of step (D) with atableting lubricant; and (F) compressing the composition of step (E)into a tablet to form a high density, fiber tablet containing about 30%to about 95% dietary fiber, based on the total weight of thecompressed-tablet fiber-composition.
 2. A method according to claim 1wherein, in step (A), the dietary fiber from the high fiber source ispresent in amounts of about 20% to about 90% by weight, based on thetotal weight of the compressed-tablet fiber-composition.
 3. A methodaccording to claim 2 wherein, in step (A), the high fiber source isselected from the group consisting of fruit fibers and grain fibers. 4.A method according to claim 3, wherein, in step (A). the high fibersource is a combination of apple fiber and corn fiber.
 5. A methodaccording to claim 2 wherein, in step (A), the microcrystallinecellulose is present in amounts of about 5% to about 75% by weight,based on the total weight of the compressed-tablet fiber-composition. 6.A method according to claim 5 wherein, in step (D), the dried product ismilled to recover granules having a particle size of about 125 to about710 microns.
 7. A method according to claim 5 wherein, in step (A), asweetening agent is additionally present.
 8. A method according to claim7 wherein, in step (D), the dried product is milled to obtain granuleshaving a particle size of about 210 to about 840 microns.
 9. A methodaccording to claim 7 wherein, in step (E), at least one flavor isadditionally present.
 10. A method according to claim 1 wherein, in step(A), the high fiber source is a combination of apple fiber and cornfiber, the dietary fiber from the high fiber source is present inamounts of about 20% to about 80% by weight; and the microcrystallinecellulose is present in amounts of about 7% to about 50% by weight,based on the total weight of the compressed-tablet fiber-composition.11. A method according to claim 10 wherein, in step (D), the driedproduct is milled to recover granules having a particles size of 149 to590 microns.
 12. A method according to claim 10 wherein, in step (D),the dried product is milled to recover granules having a particle sizeof about 250 to 840 microns.
 13. A method according to claim 10 wherein,in step (F), a high density fiber tablet containing about 35% to about90% dietary fiber is formed based on the total weight of thecompressed-tablet fiber-composition.
 14. An ingestible, high density,compressed-tablet fiber-composition prepared by:(A) blending at leastone high fiber source and a microcrystalline cellulose compression aidto form a homogenous blend; (B) mixing water with the blend of step (A)at a weight ratio of about 1.5:1 to about 2.5:1, based on the weight ofwater to the weight of the blend, for a time sufficient to form acohesive, deformable, plastic mass; (C) drying the plastic mass of step(B) to a moisture content of less than about 8% by weight, based on theweight of the dried material; (D) milling the dried product of step (C)to recover granules having a particle size of about 125 to about 840microns; (E) blending the granules of step (D) with a tabletinglubricant; and (F) compressing the composition of step (E) into a tabletto form a high density fiber tablet containing about 30% to about 95%dietary fiber, based on the total weight of the compressed-tabletfiber-composition.
 15. An ingestible, high density, compressed-tablet,fiber composition according to claim 14 wherein, in step (A), thedietary fiber from the high fiber source is present in amounts of about20% to about 80% by weight, based on the total weight of thecompressed-tablet fiber-composition.
 16. An ingestible, high density,compressed-tablet, fiber composition according to claim 15 wherein, instep (A), the high fiber source is selected from the group consisting offruit fibers and grain fibers.
 17. An ingestible, high density,compressed-tablet, fiber composition, according to claim 16 wherein, instep (A), the high fiber source is a combination of apple fiber and cornfiber.
 18. An ingestible, high density, compressed-tablet, fibercomposition according to claim 15 wherein, in step (A), themicrocrystalline cellulose is present in amounts of about 5% to about75% by weight, based on the total weight of the compressed-tabletfiber-composition.
 19. An ingestible, high density, compressed-tablet,fiber composition according to claim 18 wherein, in step (D), the driedproduct is milled to recover granules having a particles size of about125 to about 710 microns.
 20. An ingestible, high density,compressed-tablet, fiber composition according to claim 18 wherein, instep (A), a sweetening agent is additionally present.
 21. An ingestible,high denstiy, compressed-tablet, fiber-composition according to claim 20wherein, in step (D), the dried product is milled to obtain granuleshaving a particle size of about 210 to about 840 microns.
 22. Aningestible, high density, compressed-tablet, fiber-composition accordingto claim 20 wherein, in step (E), at least one flavor is additionallypresent.